Any violation in a health establishment, in an army hospital or in one of the structures mentioned in 1° to 3° of article L. 1221-10 and due to the latter, of the legislative and regulatory requirements relating to the storage of labile blood products with a view to their delivery, as well as the terms of the authorisation mentioned in the first paragraph of article L. 1221-10 , shall result in the suspension or withdrawal of this authorisation by the administrative authority. This suspension or withdrawal may only be carried out after formal notice has been given to the director of the health care organisation to take all appropriate measures to remedy the breach or failure observed, or to provide all necessary explanations. This formal notice shall be given in writing by the competent authority and shall set a time limit for compliance or response which may not exceed one month.
In an emergency involving the safety of individuals, the competent authority may suspend the authorisation as a precautionary measure.